Insights
December 9, 2024
Protected: Accelerate the path to clinic for your nasal product
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Insights
April 24, 2024
Q&A: The role of CDMOs in overcoming nasal drug delivery R&D and manufacturing challenges
Rohit Mulik, Senior Manager: Formulation R&D, and Eric Kaneps, VP, Sales & Marketing at Renaissance Lakewood LLC, answer questions about the challenges in nasal drug delivery and outline how CDMO partnerships can help to overcome them.
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Application Note
Supporting nasal product R&D and clinical manufacturing at Renaissance Learn more about the Nasal Product space and how Renaissance is making an impact.
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Insights
October 19, 2022
A Case Study on Operational Improvement
Overview: The following case study is a collaboration with Renaissance Lakewood and Raven consulting on continuous...
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Insights
October 6, 2022
Nasal spray development: Formulation and device considerations
A look at the interconnected role of the formulation, formulation excipients, and nasal spray...
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Insights
September 20, 2022
Penetration enhancers and mucoadhesives in liquid nasal spray formulations
A review of nasal spray formulation excipients and their potential for enhancing drug delivery. Test
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Insights
August 22, 2022
Understanding the Basics of Sterile Manufacturing
When developing a sterile product, people often do not understand what’s required to manufacture the product....
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Insights
August 1, 2022
What is a CDMO?
A CDMO is a Contract Development and Manufacturing Organization that accelerates how pharmaceutical companies bring drugs and therapies to market. The drug discovery to market pipeline is filled with many challenges, partnering with a CDMO lowers the risk and capital investment associated with this multi-step, multi-year, and often multi-million-dollar process.
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Insights
June 11, 2021
Nasal spray characterization and device testing
Nasal spray devices are used to deliver both locally and systemically acting pharmaceutical products,1 and are readily available in the marketplace in unit dose and metered multi-dose formats.
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